NM_004360.5(CDH1):c.2540C>G (p.Ser847Cys) AND Hereditary cancer-predisposing syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 5, 2024
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001015880.4

Allele description [Variation Report for NM_004360.5(CDH1):c.2540C>G (p.Ser847Cys)]

NM_004360.5(CDH1):c.2540C>G (p.Ser847Cys)

Gene:

CDH1:cadherin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

Preferred name:

NM_004360.5(CDH1):c.2540C>G (p.Ser847Cys)

HGVS:

NC_000016.10:g.68833390C>G
NG_008021.1:g.101099C>G
NM_001317184.2:c.2357C>G
NM_001317185.2:c.992C>G
NM_001317186.2:c.575C>G
NM_004360.5:c.2540C>GMANE SELECT
NP_001304113.1:p.Ser786Cys
NP_001304114.1:p.Ser331Cys
NP_001304115.1:p.Ser192Cys
NP_004351.1:p.Ser847Cys
LRG_301t1:c.2540C>G
LRG_301:g.101099C>G
NC_000016.9:g.68867293C>G
NM_004360.3:c.2540C>G

Protein change:

S192C

Links:

dbSNP: rs1555518249

NCBI 1000 Genomes Browser:

rs1555518249

Molecular consequence:

NM_001317184.2:c.2357C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001317185.2:c.992C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001317186.2:c.575C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_004360.5:c.2540C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Hereditary cancer-predisposing syndrome
Synonyms:: Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001176767	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 5, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001176767

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 5, 2024)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV001176767.5

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The p.S847C variant (also known as c.2540C>G), located in coding exon 16 of the CDH1 gene, results from a C to G substitution at nucleotide position 2540. The serine at codon 847 is replaced by cysteine, an amino acid with dissimilar properties. This amino acid position is well conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Based on the available evidence, the clinical significance of this variant remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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